Li Baohua, Gaudinier Allison, Tang Michelle, Taylor-Teeples Mallorie, Nham Ngoc T, Ghaffari Cyrus, Benson Darik Scott, Steinmann Margaret, Gray Jennifer A, Brady Siobhan M, Kliebenstein Daniel J
Departments of Plant Sciences (B.L., M.T., N.T.N. C.G., D.S.B., M.S., J.A.G., D.J.K.) and Plant Biology (A.G., M.T., M.T.-T., J.A.G., S.M.B.) and Genome Center (A.G., M.T., M.T.-T., J.A.G., S.M.B.), University of California, Davis, California 95616; andDynaMo Center of Excellence, University of Copenhagen, DK-1871 Frederiksberg C, Denmark (D.J.K.).
Departments of Plant Sciences (B.L., M.T., N.T.N. C.G., D.S.B., M.S., J.A.G., D.J.K.) and Plant Biology (A.G., M.T., M.T.-T., J.A.G., S.M.B.) and Genome Center (A.G., M.T., M.T.-T., J.A.G., S.M.B.), University of California, Davis, California 95616; andDynaMo Center of Excellence, University of Copenhagen, DK-1871 Frederiksberg C, Denmark (D.J.K.)
Plant Physiol. 2014 Dec;166(4):1803-20. doi: 10.1104/pp.114.248716. Epub 2014 Oct 28.
A key unanswered question in plant biology is how a plant regulates metabolism to maximize performance across an array of biotic and abiotic environmental stresses. In this study, we addressed the potential breadth of transcriptional regulation that can alter accumulation of the defensive glucosinolate metabolites in Arabidopsis (Arabidopsis thaliana). A systematic yeast one-hybrid study was used to identify hundreds of unique potential regulatory interactions with a nearly complete complement of 21 promoters for the aliphatic glucosinolate pathway. Conducting high-throughput phenotypic validation, we showed that >75% of tested transcription factor (TF) mutants significantly altered the accumulation of the defensive glucosinolates. These glucosinolate phenotypes were conditional upon the environment and tissue type, suggesting that these TFs may allow the plant to tune its defenses to the local environment. Furthermore, the pattern of TF/promoter interactions could partially explain mutant phenotypes. This work shows that defense chemistry within Arabidopsis has a highly intricate transcriptional regulatory system that may allow for the optimization of defense metabolite accumulation across a broad array of environments.
植物生物学中一个关键的未解决问题是,植物如何调节新陈代谢,以在一系列生物和非生物环境胁迫下实现性能最大化。在本研究中,我们探讨了转录调控的潜在广度,其可改变拟南芥(Arabidopsis thaliana)中防御性芥子油苷代谢物的积累。我们采用了系统的酵母单杂交研究,以鉴定与脂肪族芥子油苷途径中近21个启动子的几乎完整互补序列存在的数百种独特潜在调控相互作用。通过进行高通量表型验证,我们发现超过75%的测试转录因子(TF)突变体显著改变了防御性芥子油苷的积累。这些芥子油苷表型取决于环境和组织类型,这表明这些转录因子可能使植物能够根据当地环境调整其防御机制。此外,转录因子/启动子相互作用模式可部分解释突变体表型。这项工作表明,拟南芥中的防御化学具有高度复杂的转录调控系统,这可能有助于在广泛的环境中优化防御代谢物的积累。